Variant #0000966736 (NC_000012.11:g.117657993C>T, NM_000620.4:c.4057G>A (NOS1))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.117657993C>T
DNA change (hg38) -
Published as NOS1(NM_000620.5):c.4057G>A (p.V1353I), NOS1(NM_001204218.1):c.4159G>A (p.V1387I)
ISCN -
DB-ID NOS1_000028 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00096 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOS1 NM_000620.4 ?/. - c.4057G>A r.(?) p.(Val1353Ile)


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